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PDBsum entry 4xol

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protein metals links
Signaling protein PDB id
4xol

 

 

 

 

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JSmol PyMol  
Contents
Protein chains
74 a.a.
Metals
_ZN ×5
Waters ×10
PDB id:
4xol
Name: Signaling protein
Title: Observing the overall rocking motion of a protein in a crystal - cubic ubiquitin crystals.
Structure: Ubiquitin. Chain: a, b. Synonym: polyubiquitin-c. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: ubc. Expressed in: escherichia coli. Expression_system_taxid: 562
Resolution:
2.91Å     R-factor:   0.240     R-free:   0.269
Authors: N.Coquelle,M.Peixiang,P.Schanda,J.P.Colletier
Key ref: P.Ma et al. (2015). Observing the overall rocking motion of a protein in a crystal. Nat Commun, 6, 8361. PubMed id: 26436197 DOI: 10.1038/ncomms9361
Date:
16-Jan-15     Release date:   14-Oct-15    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
P0CG48  (UBC_HUMAN) -  Polyubiquitin-C from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
685 a.a.
74 a.a.
Key:    PfamA domain  Secondary structure

 Enzyme reactions 
   Enzyme class: E.C.?
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]

 

 
DOI no: 10.1038/ncomms9361 Nat Commun 6:8361 (2015)
PubMed id: 26436197  
 
 
Observing the overall rocking motion of a protein in a crystal.
P.Ma, Y.Xue, N.Coquelle, J.D.Haller, T.Yuwen, I.Ayala, O.Mikhailovskii, D.Willbold, J.P.Colletier, N.R.Skrynnikov, P.Schanda.
 
  ABSTRACT  
 
The large majority of three-dimensional structures of biological macromolecules have been determined by X-ray diffraction of crystalline samples. High-resolution structure determination crucially depends on the homogeneity of the protein crystal. Overall 'rocking' motion of molecules in the crystal is expected to influence diffraction quality, and such motion may therefore affect the process of solving crystal structures. Yet, so far overall molecular motion has not directly been observed in protein crystals, and the timescale of such dynamics remains unclear. Here we use solid-state NMR, X-ray diffraction methods and μs-long molecular dynamics simulations to directly characterize the rigid-body motion of a protein in different crystal forms. For ubiquitin crystals investigated in this study we determine the range of possible correlation times of rocking motion, 0.1-100 μs. The amplitude of rocking varies from one crystal form to another and is correlated with the resolution obtainable in X-ray diffraction experiments.
 

 

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